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209864

Sigma-Aldrich

4-tert-Butylaniline

99%

Sinônimo(s):

4-(1,1-Dimethylethyl)aniline, 4-(1,1-Dimethylethyl)benzenamine, 4-Amino-tert-butylbenzene, 4-t-Butylphenylamine, 4-tert-Butylbenzenamine, 4-tert-Butylphenylamine, p-(tert-Butyl)phenylamine, p-tert-Butylaniline

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About This Item

Fórmula linear:
(CH3)3CC6H4NH2
Número CAS:
769-92-6
Peso molecular:
149.23
Beilstein:
2205786
Número CE:
212-215-9
Número MDL:
MFCD00007899
Código UNSPSC:
12352100
ID de substância PubChem:
24852597
NACRES:
NA.22

Nível de qualidade

100

Ensaio

99%

forma

liquid

índice de refração

n20/D 1.538 (lit.)

pb

90-93 °C/3 mmHg (lit.)

pf

15-16 °C (lit.)

densidade

0.937 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC(C)(C)c1ccc(N)cc1

InChI

1S/C10H15N/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,11H2,1-3H3

chave InChI

WRDWWAVNELMWAM-UHFFFAOYSA-N

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Descrição geral

Schiff base formation reaction between 4-tert-butylaniline and 4-tert-butylbenzaldehyde in ethanol has been carried out using the matrix-assisted laser desorption ionization-chip system.

Aplicação

4-tert-Butylaniline was used in the synthesis of:
  • 4-tert-Butyl-4′,4″-dinitrotriphenylamine, new triphenylamine-containing diamine monomer
  • 2-oxopyrimido[4,5-d]pyrimidin-5(6H)-one

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

215.6 °F - closed cup

Ponto de fulgor (°C)

102 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
STBF5396V
STBB7541V
S35756V
STBB7541
05712HH

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Self-complementary hydrogen bonding heterocycles designed for the enforced self-assembly into supramolecular macrocycles.
Marsh A, et al.
Chemical Communications (Cambridge, England), 13, 1527-1528 (1996)
Christopher G Thomson et al.
Bioorganic & medicinal chemistry letters, 21(14), 4281-4283 (2011-06-15)
A novel and robust synthesis of the fragment, 2-amino-5-tert-butylpyridine, has been described, which has been shown to have improved physicochemical properties over 4-tert-butylaniline, when considering drug-like properties. The synthesis also yields fragments containing more highly oxidised precursors to the tert-butyl
Novel aromatic polyamides and polyimides functionalized with 4-tert-butyltriphenylamine groups.
Hsiao S-H, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(15), 4579-4592 (2006)
Monica Brivio et al.
Lab on a chip, 5(4), 378-381 (2005-03-26)
The integration of a monitoring port along the microfluidic path of a MALDI-chip integrated device is described. Optimization of the microreactor design allows longer reaction and measuring times. The Schiff base reaction between 4-tert-butylaniline (1) and 4-tert-butylbenzaldehyde (2) in ethanol
Ji Han Kim et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(38), 9060-9070 (2019-04-16)
Organic light-emitting diodes are currently under research to achieve high efficiency and long life by using thermally activated delayed fluorescence (TADF) materials. In particular, many studies have focused on ensuring high efficiency in fluorescent devices by introducing TADF materials. Herein

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